Affiliation:
1. Institute of Medical Microbiology, University of Oslo, Oslo, Norway,1 and
2. Department of Medical Microbiology, Vrije Universiteit, Amsterdam,2 The Netherlands
3. Department of Enzymology and Protein Engineering, Utrecht University, Utrecht,3 and
Abstract
ABSTRACT
Previously, we have shown that
Helicobacter pylori
can spontaneously and reversibly change its membrane lipid composition, producing variants with low or high content of lysophospholipids. The “lyso” variant contains a high percentage of lysophospholipids, adheres better to epithelial cells, and releases more proteins such as urease and VacA, compared to the “normal” variant, which has a low content of lysophospholipids. Prolonged growth of the normal variant at pH 3.5, but not under neutral conditions, leads to enrichment of lyso variant colonies, suggesting that the colony switch is relevant to acid adaptation. In this study we show that the change in membrane lipid composition is due to phase variation in the
pldA
gene. A change in the (C) tract length of this gene results in reversible frameshifts, translation of a full-length or truncated
pldA
, and the production of active or inactive outer membrane phospholipase A (OMPLA). The role of OMPLA in determining the colony morphology was confirmed by the construction of an OMPLA-negative mutant. Furthermore, variants with an active OMPLA were able to survive acidic conditions better than variants with the inactive form. This explains why the lyso variant is selected at low pH. Our studies demonstrate that phase variation in the
pldA
gene, resulting in an active form of OMPLA, is important for survival under acidic conditions. We also demonstrated the active OMPLA genotype in fresh isolates of
H. pylori
from patients referred to gastroscopy for dyspepsia.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
52 articles.
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